467 related articles for article (PubMed ID: 17995939)
1. CHL1 promotes Sema3A-induced growth cone collapse and neurite elaboration through a motif required for recruitment of ERM proteins to the plasma membrane.
Schlatter MC; Buhusi M; Wright AG; Maness PF
J Neurochem; 2008 Feb; 104(3):731-44. PubMed ID: 17995939
[TBL] [Abstract][Full Text] [Related]
2. Binding partners L1 cell adhesion molecule and the ezrin-radixin-moesin (ERM) proteins are involved in development and the regenerative response to injury of hippocampal and cortical neurons.
Haas MA; Vickers JC; Dickson TC
Eur J Neurosci; 2004 Sep; 20(6):1436-44. PubMed ID: 15355311
[TBL] [Abstract][Full Text] [Related]
3. Semaphorin3A regulates axon growth independently of growth cone repulsion via modulation of TrkA signaling.
Ben-Zvi A; Ben-Gigi L; Yagil Z; Lerman O; Behar O
Cell Signal; 2008 Mar; 20(3):467-79. PubMed ID: 18096366
[TBL] [Abstract][Full Text] [Related]
4. Close homolog of L1 modulates area-specific neuronal positioning and dendrite orientation in the cerebral cortex.
Demyanenko GP; Schachner M; Anton E; Schmid R; Feng G; Sanes J; Maness PF
Neuron; 2004 Oct; 44(3):423-37. PubMed ID: 15504324
[TBL] [Abstract][Full Text] [Related]
5. Single-chain variable fragment antibodies against the neural adhesion molecule CHL1 (close homolog of L1) enhance neurite outgrowth.
Dong L; Chen S; Richter M; Schachner M
J Neurosci Res; 2002 Aug; 69(4):437-47. PubMed ID: 12210838
[TBL] [Abstract][Full Text] [Related]
6. Semaphorin 3A inhibits ERM protein phosphorylation in growth cone filopodia through inactivation of PI3K.
Gallo G
Dev Neurobiol; 2008 Jun; 68(7):926-33. PubMed ID: 18327764
[TBL] [Abstract][Full Text] [Related]
7. Semaphorin3A-induced receptor endocytosis during axon guidance responses is mediated by L1 CAM.
Castellani V; Falk J; Rougon G
Mol Cell Neurosci; 2004 May; 26(1):89-100. PubMed ID: 15121181
[TBL] [Abstract][Full Text] [Related]
8. Close homologue of adhesion molecule L1 promotes survival of Purkinje and granule cells and granule cell migration during murine cerebellar development.
Jakovcevski I; Siering J; Hargus G; Karl N; Hoelters L; Djogo N; Yin S; Zecevic N; Schachner M; Irintchev A
J Comp Neurol; 2009 Apr; 513(5):496-510. PubMed ID: 19226508
[TBL] [Abstract][Full Text] [Related]
9. Depolarization recruits DCC to the plasma membrane of embryonic cortical neurons and enhances axon extension in response to netrin-1.
Bouchard JF; Horn KE; Stroh T; Kennedy TE
J Neurochem; 2008 Oct; 107(2):398-417. PubMed ID: 18691385
[TBL] [Abstract][Full Text] [Related]
10. Neural cell adhesion molecule-180-mediated homophilic binding induces epidermal growth factor receptor (EGFR) down-regulation and uncouples the inhibitory function of EGFR in neurite outgrowth.
Povlsen GK; Berezin V; Bock E
J Neurochem; 2008 Feb; 104(3):624-39. PubMed ID: 17995934
[TBL] [Abstract][Full Text] [Related]
11. Evidence that Sema3A and Sema3F regulate the migration of GABAergic neurons in the developing neocortex.
Tamamaki N; Fujimori K; Nojyo Y; Kaneko T; Takauji R
J Comp Neurol; 2003 Jan; 455(2):238-48. PubMed ID: 12454988
[TBL] [Abstract][Full Text] [Related]
12. Differential expression of ezrin/radixin/moesin (ERM) and ERM-associated adhesion molecules in the blastocyst and uterus suggests their functions during implantation.
Matsumoto H; Daikoku T; Wang H; Sato E; Dey SK
Biol Reprod; 2004 Mar; 70(3):729-36. PubMed ID: 14613898
[TBL] [Abstract][Full Text] [Related]
13. Neurite outgrowth triggered by the cell adhesion molecule L1 requires activation and inactivation of the cytoskeletal protein cofilin.
Figge C; Loers G; Schachner M; Tilling T
Mol Cell Neurosci; 2012 Feb; 49(2):196-204. PubMed ID: 22019611
[TBL] [Abstract][Full Text] [Related]
14. Response of radixin to perturbations of growth cone morphology and motility in chick sympathetic neurons in vitro.
Gonzalez-Agosti C; Solomon F
Cell Motil Cytoskeleton; 1996; 34(2):122-36. PubMed ID: 8769724
[TBL] [Abstract][Full Text] [Related]
15. Semaphorin 3A displays a punctate distribution on the surface of neuronal cells and interacts with proteoglycans in the extracellular matrix.
De Wit J; De Winter F; Klooster J; Verhaagen J
Mol Cell Neurosci; 2005 May; 29(1):40-55. PubMed ID: 15866045
[TBL] [Abstract][Full Text] [Related]
16. Nerve growth factor, glial cell line-derived neurotrophic factor and neurturin prevent semaphorin 3A-mediated growth cone collapse in adult sensory neurons.
Wanigasekara Y; Keast JR
Neuroscience; 2006 Oct; 142(2):369-79. PubMed ID: 16876331
[TBL] [Abstract][Full Text] [Related]
17. L1 and CHL1 Cooperate in Thalamocortical Axon Targeting.
Demyanenko GP; Siesser PF; Wright AG; Brennaman LH; Bartsch U; Schachner M; Maness PF
Cereb Cortex; 2011 Feb; 21(2):401-12. PubMed ID: 20576928
[TBL] [Abstract][Full Text] [Related]
18. Sema3A regulates the timing of target contact by cranial sensory axons.
Dillon TE; Saldanha J; Giger R; Verhaagen J; Rochlin MW
J Comp Neurol; 2004 Feb; 470(1):13-24. PubMed ID: 14755522
[TBL] [Abstract][Full Text] [Related]
19. The generation of localized calcium rises mediated by cell adhesion molecules and their role in neuronal growth cone motility.
Dunican DJ; Doherty P
Mol Cell Biol Res Commun; 2000 May; 3(5):255-63. PubMed ID: 10964748
[TBL] [Abstract][Full Text] [Related]
20. Cell adhesion molecule L1 modulates nerve-growth-factor-induced CGRP-IR fiber sprouting.
Chaudhry N; de Silva U; Smith GM
Exp Neurol; 2006 Nov; 202(1):238-49. PubMed ID: 16860320
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]